Party Petra, Klement Márk László, Gaudio Bianca Maria, Sorrenti Milena, Ambrus Rita
Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, 6720 Szeged, Hungary.
Department of Drug Sciences, University of Pavia, 27100 Pavia, Italy.
Pharmaceutics. 2025 Apr 7;17(4):486. doi: 10.3390/pharmaceutics17040486.
: Ciprofloxacin (CIP) is a poorly water-soluble fluoroquinolone-type antibiotic that can be useful in the treatment of lung infections. When the drugs are delivered directly to the lungs, a smaller dosage is needed to achieve the desired effect compared to the oral administration. Moreover, the application of nanoparticles potentially enhances the effectiveness of the treatments while lowering the possible side effects. Therefore, we aimed to develop a "nano-in-micro" structured dry powder inhaler formulation containing CIP. : A two-step preparation method was used. Firstly, a nanosuspension was first prepared using a high-performance planetary mill by wet milling. After the addition of different additives (leucine and mannitol), the solid formulations were created by spray drying. The prepared DPI samples were analyzed by using laser diffraction, nanoparticle tracking analysis, scanning electron microscopy, X-ray powder diffraction, and differential scanning calorimetry. The solubility and in vitro dissolution tests in artificial lung fluid and in vitro aerodynamic investigations (Spraytec device, Andersen Cascade Impactor) were carried out. : The nanosuspension (D50: 140.0 ± 12.8 nm) was successfully prepared by the particle size reduction method. The DPIs were suitable for inhalation based on the particle diameter and their spherical shape. Improved surface area and amorphization after the preparation processes led to faster drug release. The excipient-containing systems were characterized by large lung deposition (fine particle fraction around 40%) and suitable aerodynamic diameter (between 3 and 4 µm). : We have successfully formulated a nanosized antibiotic-containing formulation for pulmonary delivery, which could provide a potential treatment for patients with different respiratory infections.
环丙沙星(CIP)是一种水溶性较差的氟喹诺酮类抗生素,可用于治疗肺部感染。与口服给药相比,当药物直接输送到肺部时,达到预期效果所需的剂量更小。此外,纳米颗粒的应用可能会提高治疗效果,同时降低可能的副作用。因此,我们旨在开发一种含有环丙沙星的“纳米包微米”结构的干粉吸入剂制剂。
采用两步制备方法。首先,使用高性能行星式球磨机通过湿磨制备纳米混悬液。加入不同的添加剂(亮氨酸和甘露醇)后,通过喷雾干燥制备固体制剂。使用激光衍射、纳米颗粒跟踪分析、扫描电子显微镜、X射线粉末衍射和差示扫描量热法对制备的干粉吸入剂样品进行分析。进行了在人工肺液中的溶解度和体外溶出试验以及体外空气动力学研究(Spraytec装置、安德森撞击器)。
通过粒径减小法成功制备了纳米混悬液(D50:140.0±12.8nm)。基于粒径及其球形形状,干粉吸入剂适合吸入。制备过程后表面积的改善和非晶化导致药物释放更快。含辅料的体系具有较大的肺部沉积率(细颗粒分数约为40%)和合适的空气动力学直径(3至4μm之间)。
我们成功地制备了一种用于肺部给药的含纳米抗生素制剂,可为不同呼吸道感染患者提供潜在的治疗方法。